drugset / Trial / NCT00873561

A Study to Evaluate NBI-6024 in Adult and Adolescent Patients With New Onset of Type 1 Diabetes Mellitus

NCT00873561 ↗

Phase 1 Completed 188 enrolled Neurocrine Biosciences
RandomizedParallel-groupDouble-blindBasic science

Summary

This was a study designed to evaluate the efficacy of multiple doses of an investigational drug, NBI-6024, in adult (18 to 35 years of age) and adolescent (10 to 17 years of age) patients with new onset type 1 diabetes mellitus, on endogenous insulin production. A total of 188 patients were enrolled in the study. The study was divided into three periods: screening, treatment (comprising an induction phase and maintenance phase), and follow-up. NBI-6024 was generally well tolerated and exhibits a benign safety profile, as there were no significant safety issues with NBI-6024 treatment. In summary, NBI-6024 did not demonstrate statistically significant efficacy compared with placebo.

Timeline

Start
2001-12
Primary completion
2006-04
Completion
2006-07

Drugs

EvaluationDrugModalityDoseRoute
Comparator NBI-6024 Peptide 0.1 mg Subcutaneous
Comparator NBI-6024 Peptide 0.5 mg Subcutaneous
Comparator NBI-6024 Peptide 1 mg Subcutaneous